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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05533281
Other study ID # Nausea and vomiting
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date September 15, 2022
Est. completion date November 3, 2023

Study information

Verified date December 2022
Source The Second Affiliated Hospital of Chongqing Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To explore the effect of commonly used antiemetic drugs on reducing nausea and vomiting caused by intravenous tramadol injection, so as to reduce the incidence of nausea and vomiting in clinical use of tramadol and provide guidance for the clinical use of tramadol injection


Recruitment information / eligibility

Status Completed
Enrollment 200
Est. completion date November 3, 2023
Est. primary completion date October 30, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - American Society of Anesthesiologists classification I-II - 18.5=BMI=28 - Patients who receiving breast and thyroid surgery and requiring general anesthesia and receive PCIA - Voluntarily and be able to understand and sign the informed consent form Exclusion Criteria: - Long-term use of analgesics, psychotropic drugs (including opioids, NSAIDS, antidepressants) history - History of allergy to opioids - Patients with a history or family history of epilepsy that has not been controlled by treatment - Sedatives and antidepressants were used 24 hours before surgery - Failure to cooperate with the study for any reason or in the opinion of the investigator

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
tropisetron
One tropisetron was given 30 minutes in advance, and then tramadol 1.5mg/kg was intravenously injected with a micropump at a constant speed.
metoclopramide
One dose of metoclopramide was given 30 minutes in advance, and then tramadol 1.5mg/kg was injected intravenously with a micropump at a constant speed.
dexamethasone
One dose of dexamethasone was given 30 minutes in advance, and then tramadol 1.5mg/kg was injected intravenously with a micropump at a constant speed.
Other:
normal saline
Equal dose of normal saline was given 30 minutes in advance, and then tramadol 1.5mg/kg was injected intravenously with a micropump at a constant speed.

Locations

Country Name City State
China The Second Affiliated Hospital, Chongqing Medical University Chongqing Chongqing

Sponsors (1)

Lead Sponsor Collaborator
The Second Affiliated Hospital of Chongqing Medical University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary NRS score of nausea and vomiting NRS score of nausea and vomiting was assessed by numerical rating scale (0-10, 0 representing no nausea and 10 the worst nausea imaginable) From before administration to 10min after administration
Secondary Incidence of postoperative nausea and vomiting PONV is recorded according to whether the patient present nausea and vomiting during the follow-up visits after surgery From end of operation to 24 hours after operation
Secondary NRS score of postoperative nausea and vomiting NRS score of nausea and vomiting was assessed by numerical rating scale (0-10, 0 representing no nausea and 10 the worst nausea imaginable) From end of operation to 24 hours after operation
Secondary Incidence of extra treatment for postoperative nausea and vomiting Incidence of extra treatment for postoperative nausea and vomiting was assessed by whether patient using other treatment for postoperative nausea and vomiting during the the follow-up visits after surgery From end of operation to 24 hours after operation
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